<p>Fitness was measured in competition with cooperating bacteria at initially low (c.5%) and high (c.50%) cheat frequency. Diamonds show medians and associated 95% confidence intervals.</p
Hamilton's inclusive fitness theory provides a leading explanation for the problem of cooperation. A...
Measuring fitness with precision is a key issue in evolutionary biology, particularly in studying mu...
<p><b>A</b>) Relative fitness of the 21 viable mutants in CEMx174 cells. Values shown are an average...
<p>A) The resolution of our assay was assessed by performing 64 competitions of wild-type spores fro...
<p>The Δ4904 single mutant was outcompeted by the wild type. <b>Panels A, B</b> and <b>C</b> depict ...
<p>Fitness (mean ± SD; <i>n</i> = 4) of antibiotic-resistant mutants generated by <i>ΔmutY</i> (circ...
Results of competition experiments designed to estimate fitness of evolved E. coli clones relative t...
<p>Fitness of the sweeper was determined by competition against a single competitor (lowest level of...
Bacteria perform cooperative behaviours that are exploitable by non-cooperative cheats, and cheats f...
The relative fitness of viral variants has previously been defined as the slope of the logarithmic r...
We describe a sensitive, internally controlled method for comparing the genetic adaptability and rel...
Competitive fitness measurements for 46 evolved populations of Escherichia coli. Three replicate fit...
<p>Correlation of mean (±SE) fitness estimates from eight genotype pairs estimated with two differen...
<p>Mean mutation frequency (± 95% confidence interval) was assayed for wild-type ϕ6 (ANC), and for o...
<p>The competitive fitness of MN8m in co-culture with PNAG-negative, non-mucoid JB12 was determined ...
Hamilton's inclusive fitness theory provides a leading explanation for the problem of cooperation. A...
Measuring fitness with precision is a key issue in evolutionary biology, particularly in studying mu...
<p><b>A</b>) Relative fitness of the 21 viable mutants in CEMx174 cells. Values shown are an average...
<p>A) The resolution of our assay was assessed by performing 64 competitions of wild-type spores fro...
<p>The Δ4904 single mutant was outcompeted by the wild type. <b>Panels A, B</b> and <b>C</b> depict ...
<p>Fitness (mean ± SD; <i>n</i> = 4) of antibiotic-resistant mutants generated by <i>ΔmutY</i> (circ...
Results of competition experiments designed to estimate fitness of evolved E. coli clones relative t...
<p>Fitness of the sweeper was determined by competition against a single competitor (lowest level of...
Bacteria perform cooperative behaviours that are exploitable by non-cooperative cheats, and cheats f...
The relative fitness of viral variants has previously been defined as the slope of the logarithmic r...
We describe a sensitive, internally controlled method for comparing the genetic adaptability and rel...
Competitive fitness measurements for 46 evolved populations of Escherichia coli. Three replicate fit...
<p>Correlation of mean (±SE) fitness estimates from eight genotype pairs estimated with two differen...
<p>Mean mutation frequency (± 95% confidence interval) was assayed for wild-type ϕ6 (ANC), and for o...
<p>The competitive fitness of MN8m in co-culture with PNAG-negative, non-mucoid JB12 was determined ...
Hamilton's inclusive fitness theory provides a leading explanation for the problem of cooperation. A...
Measuring fitness with precision is a key issue in evolutionary biology, particularly in studying mu...
<p><b>A</b>) Relative fitness of the 21 viable mutants in CEMx174 cells. Values shown are an average...